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- 2014
Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia
Houten, S. M., Denis, S., te Brinke, H., Jongejan, A., van Kampen, A. H. C., Bradley, E. J., Baas, F., Hennekam, R. C. M., Millington, D. S., Young, S. P., Frazier, D. M., Gucsavas-Calikoglu, M. & Wanders, R. J. A., 2014, In: Human molecular genetics. 23, 18, p. 5009-5016Research output: Contribution to journal › Article › Academic › peer-review
Mitochondrial protein acetylation is driven by acetyl-CoA from fatty acid oxidation
Pougovkina, O., te Brinke, H., Ofman, R., van Cruchten, A. G., Kulik, W., Wanders, R. J. A., Houten, S. M. & de Boer, V. C. J., 2014, In: Human molecular genetics. 23, 13, p. 3513-3522Research output: Contribution to journal › Article › Academic › peer-review
- 2013
Carnitine palmitoyltransferase 2 and carnitine/acylcarnitine translocase are involved in the mitochondrial synthesis and export of acylcarnitines
Violante, S., Ijlst, L., te Brinke, H., Tavares de Almeida, I., Wanders, R. J. A., Ventura, F. V. & Houten, S. M., 2013, In: FASEB journal. 27, 5, p. 2039-2044Research output: Contribution to journal › Article › Academic › peer-review
Genetic basis of hyperlysinemia
Houten, S. M., te Brinke, H., Denis, S., Ruiter, J. P., Knegt, A. C., de Klerk, J. B., Augoustides-Savvopoulou, P., Häberle, J., Baumgartner, M. R., Coşkun, T., Zschocke, J., Sass, J. O., Poll-The, B. T., Wanders, R. J. & Duran, M., 2013, In: Orphanet journal of rare diseases. 8, 1, p. 57Research output: Contribution to journal › Article › Academic › peer-review
Impaired amino acid metabolism contributes to fasting-induced hypoglycemia in fatty acid oxidation defects
Houten, S. M., Herrema, H., te Brinke, H., Denis, S., Ruiter, J. P. N., van Dijk, T. H., Argmann, C. A., Ottenhoff, R., Müller, M., Groen, A. K., Kuipers, F., Reijngoud, D-J. & Wanders, R. J. A., 2013, In: Human molecular genetics. 22, 25, p. 5249-5261Research output: Contribution to journal › Article › Academic › peer-review
Peroxisomes contribute to the acylcarnitine production when the carnitine shuttle is deficient
Violante, S., Ijlst, L., te Brinke, H., Koster, J., Tavares de Almeida, I., Wanders, R. J. A., Ventura, F. V. & Houten, S. M., 2013, In: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS. 1831, 9, p. 1467-1474Research output: Contribution to journal › Article › Academic › peer-review
- 2012
Functional redundancy of mitochondrial enoyl-CoA isomerases in the oxidation of unsaturated fatty acids
van Weeghel, M., te Brinke, H., van Lenthe, H., Kulik, W., Minkler, P. E., Stoll, M. S. K., Sass, J. O., Janssen, U., Stoffel, W., Schwab, K. O., Wanders, R. J. A., Hoppel, C. L. & Houten, S. M., 2012, In: FASEB journal. 26, 10, p. 4316-4326Research output: Contribution to journal › Article › Academic › peer-review
- 2011
Differential effects of short- and long-term high-fat diet feeding on hepatic fatty acid metabolism in rats
Ciapaite, J., van den Broek, N. M., te Brinke, H., Nicolay, K., Jeneson, J. A., Houten, S. M. & Prompers, J. J., 2011, In: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS. 1811, 7-8, p. 441-451Research output: Contribution to journal › Article › Academic › peer-review
- 2009
Pyruvate dehydrogenase kinase 4 expression is synergistically induced by AMP-activated protein kinase and fatty acids
Houten, S. M., Chegary, M., te Brinke, H., Wijnen, W. J., Glatz, J. F. C., Luiken, J. J. F. P., Wijburg, F. A. & Wanders, R. J. A., 2009, In: Cellular and molecular life sciences. 66, 7, p. 1283-1294Research output: Contribution to journal › Article › Academic › peer-review
- 2008
Characterization of L-aminocarnitine, an inhibitor of fatty acid oxidation
Chegary, M., te Brinke, H., Doolaard, M., Ijlst, L., Wijburg, F. A., Wanders, R. J. A. & Houten, S. M., 2008, In: Molecular genetics and metabolism. 93, 4, p. 403-410Research output: Contribution to journal › Article › Academic › peer-review
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